Data from 262 samples were analyzed (249 myeloma patients and 13

Data from 262 samples were analyzed (249 myeloma patients and 13 other diagnoses): 100 consecutively thawed samples with a storage time of < 1 year (all 10% DMSO), 50 consecutive samples stored for 1-4.9 years (10% DMSO),

50 samples stored for 5-9 years (5% DMSO) and all samples stored and used for transplant after > 9 years (60 samples, 5% DMSO; two samples, 10% DMSO). Results. No statistically significant difference in viability between the 5% DMSO and 10% DMSO groups was observed (P = 0.08), OICR-9429 in vitro so the 1-4.9 years and 5-9 years were combined and the three groups (< 1 year, 1-9 years and > 9 years) were compared using an anova test. There was no difference in viability based on cryostorage period (P = 0.23) or between myeloma and other diagnoses (P = 0.45). No difference was seen in time to White blood cell (WBC) engraftment (P = 0.10) or to platelet engraftment between groups (P = 0.52). Conclusions. These data suggest that long-term storage in 5% DMSO and human serum albumin is safe.”
“Cytochrome c(5) of pressure-sensitive Shewanella livingstonensis (SL cytc(5)) exhibits lower thermal stability than

a highly homologous counterpart of pressure-tolerant Shewanella violacea. This stability difference is due to an enthalpic effect that can be attributed to the amino acid residue at position 50 (Leu or Lys). These cytc(5) proteins are appropriate materials for understanding the protein stability mechanism.”
“To determine selleck chemicals the mechanism of aluminum (Al) detoxification in the roots of tea plants (Camellia sinensis (L.) Kuntze), the amounts of Al and Al-chelating compounds (fluoride (F), organic acids and catechins) were measured and the chemical forms of A, in root cell extracts were identified by the application of Al-27-nuclear magnetic resonance (NMR) spectroscopy. Tea plants were cultivated in nutrient GDC-0973 supplier solutions containing 0, 4, 1.0 and 4.0 mM of Al at pH 4.2 for approximately 10 weeks. The levels of soluble Al, water-soluble oxalate and citrate, but not F, malate or catechins in young roots

increased with an increase in the concentration of Al in the treatment solution. The Al-27 NMR spectra of root tips and cell sap extracted from root tips that had been treated with Al were almost identical and had four signals, with two (11 and 16 ppm) apparently corresponding to the known chemical shifts of Al-oxalate complexes. In the spectra of cell sap, the resonances at 11 and 16 ppm increased with an increase in the Al contents. These results suggest that the levels of Al-oxalate complexes increased in response to an increase in the Al level, implying that oxalate is a key Al-chelating compound in the mechanism of Al detoxification in the tea root. (C) 2007 Elsevier Ltd. All rights reserved.”
“To the Editor: In their Perspective article, Morain et al. (Aug.

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